Author

Aparna Dhondi Dalvi

Indian Council of Medical ResearchORCID 0009-0007-6972-6474Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abhinav K. JainiD· 1 shared Anoop KumariD· 1 shared Athulya EdavazhippurathiD· 1 shared Atul KashyapiD· 1 shared Geeta Madathil GovindarajiD· 1 shared Krishnan Chakkiyar· 1 shared Manisha Rajan MadkaikariD· 1 shared Mohamed ImraniD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Abhinav K. JainORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Whole Genome Sequencing identifies novel structural variant in a large Indian family affected with X - linked agammaglobulinemia

Abhinav K. Jain, Geeta Madathil Govindaraj, Athulya Edavazhippurath, Nabeel Valappil Faisal, Rahul C. Bhoyar, Vishu Gupta, Ramya Uppuluri, Shiny Padinjarayil Manakkad, Atul Kashyap, Anoop Kumar, Mohit Kumar Divakar, Mohamed Imran, Sneha Sawant, Aparna Dhondi Dalvi, Krishnan Chakkiyar, , Vinod Scaria

The paper identifies a novel 5,296 bp deletion in the BTK gene in an Indian family with X-linked agammaglobulinemia through whole genome sequencing and carrier screening.

PLoS ONE · Jul 12, 2021Peer-reviewedGenetic & Genomic Medicine